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Characteristics of a liposome immunoassay on a poly(methyl methacrylate) surface
Authors:Sang Youn Hwang  Yoichi Kumada  Gi Hoon Seong  Jaebum Choo  Shigeo Katoh  Eun Kyu Lee
Institution:(1) Department of Chemical Engineering, Hanyang University, Ansan, South Korea;(2) Department of Chemistry and Materials Technology, Kyoto Institute of Technology, Kyoto, Japan;(3) Department of Applied Chemistry, Hanyang University, Ansan, South Korea;(4) Department of Chemical Science and Engineering, Kobe University, Kobe, Japan
Abstract:Liposome immunoassay (LIA) is based on enzyme immunoassay (EIA) but the detection sensitivity could be significantly enhanced by using antibody-coupled immunoliposomes encapsulating HRP (horse radish peroxidase). Here, we applied LIA to non-porous poly(methyl methacrylate) (PMMA) and polystyrene (PS) surfaces to compare its detection sensitivity with that of EIA, using rabbit IgG (a ligand molecule) and anti-rabbit IgG antibody (a capture molecule) as the model system. LIA developed much stronger color signals than EIA, especially at a lower concentration range (< ca. 1 μg mL−1). PMMA showed higher affinity toward rabbit IgG than the PS surface, and the anti-rabbit IgG antibody adsorbed on PMMA was more stable than that on PS. Furthermore, the effects of spot volume and antibody concentration on the signal density were analyzed. The signal density increased as the antibody concentration increased, but it was not significantly affected by the spot volume (2.5–20 μL). In conclusion, LIA on PMMA as a solid support is a very useful, highly sensitive microarray detection system. Sang Youn Hwang and Yoichi Kumada have same rights on this paper.
Keywords:Liposome immunoassay  Immunoliposome  PMMA  Microarray detection  Signal enhancement
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